Tetrahydroquinoxalinyl phosphates or thiophosphates



United States Patent 3,505,327 TETRAHYDROQUINOXALINYL PHOSPHATES 0R THIOPHOSPHATES Bernard Miller, Princeton, and Tamara Helen Mladineo Gund, Elizabeth, N.J., assignors to American Cyanamid Company, Stamford, Conn., a corporation of Maine No Drawing. Filed Aug. 7, 1967, Ser. No. 658,637 Int. Cl. C07d 51/00, 57/00 wherein X is a sulfur or an oxygen atom, R and R are each lower alkyl, lower alkoxy, lower thioalkyl, aryl, aralkyl or NR R R is hydrogen or lower alkyl, and R and R are each hydrogen and lower alkyl, useful in controlling insects and arachnids which damage agronomic crops.

The present invention relates to new tetrahydroquinoxalinyl phosphates, thiophosphates and the like, a method for the preparation thereof, and to a method of controlling insects and arachnids therewith. More particularly, it is concerned with a compound of the formula:

0,0-diethyl 0,5 ,6,7 ,8,-tetrahydro-6 (7 -methyl-2quinoxalinyl phosphorothioate,

0,0-dimethyl 0-5,6,7,8-tetrahydro-Z-quinoxalinyl phosphorothioate,

0,0-diisopropyl 5,6,7,8-tetrahydro-2-quinoxalinyl phosphorothioate,

Diisopropyl 5,6,7,S-tetrahydro-2-quinoxalinyl phosphate,

0,0-diethyl O-5,6,7,8-tetrahydro-2-quinoxalinyl phosphorothioate,

O-ethyl O-methyl O-5,6,7,8-tetrahydro-Z-quinoxalinyl phosphorothioate,

N,N-dimethyl-O-ethyl O-5,6,7,8-tetrahydro-2-quinoxaliny1 phosphoroamidothioate,

O-ethyl O-5,6,7,8-tetrahydro-6 (7) -methyl-2-quinoxalinyl phenylphosphonothiate 3,505,327 Patented Apr. 7, 1970 O,S-dimethy1 O-5,6,7,8-tetrahyd ro-2-quinoxalinyl phosphorodithioate, O-ethyl-O-5,6,7,8-tetrahydro-2-quinoxalinyl phonate, S,S-dimethyl O-5,6,7,8-tetrahydro-2-quinoxalinyl phorodithioate, O-isoprOpyl O-methyl linyl phosphorothioate, Diethyl 5,6,7,8-tetrahydro-2-quinoxalinyl phosphate and 0,0-dipropyl 0-5,6,7,8-tetrahydroquinoxalinyl phosphorothioate.

ethanephosphos- O-5,6,7,8-tetrahydro-2-quinoxa- The compounds of the invention can be synthesized in a straightforward and economical manner by effecting a reaction between a tetrahydroquinoxaline and a phosphorus-containing ester halide in the presence of a strong base. The overall reaction may :be graphically written as follows:

wherein Y is halogen, such as chlorine or bromine; X is sulfur or oxygen; R and R are each selected from the group consisting of lower alkyl, lower alkoxy, lower thioalkyl, NR R and aryl, such as phenyl or halophenyl, and alkaryl, such as benzyl; and R is hydrogen or lower alkyl; and R and R are each selected from the group consisting of hydrogen and lower alkyl. Preferably, the reaction is carried out in the presence of an inert solvent, such as t-butanol, dimethylsulfoxide, dimethylformamide or water over a wide-range of temperatures, usually between about 0 C. and C. Among the strong bases which are useful in the process are sodium and potassium t-butoxide, sodium and potassium hydroxide and tertiary amines, such as trimethylamine.

The tetrahydroquinoxalines can be conveniently prepared by initially halogenating a cyclohexanone. The reaction is carried out in the presence of an acid, such as glacial acetic acid, and the overall reaction is shown by the following graphic equation:

wherein X is either chlorine or bromine. The halogenated cyclohexanone may then be treated with aqueous ferric chloride solution at an elevated temperature, preferably at "boiling, to give a cyclohexanedione, which is next treated with a glycinamide hydrohalide, such as glycinamide hydrochloride, at from 0 to 100 C. in the presence of a suitable base to yield the desired tetrahydroquinoxaline. The reaction is graphically illustrated as:

tell.

i Ra L I An illustrative tetrahydroquinoxaline reactant for Reaction [I] above is:

2-oxy-5 ,6,7,8-tetrahydro quin oxaline, 6 (7 -methyl-2-oxy-5,6,7,8-tetrahydroquinoxaline, and 6 (7) -ethyl-2-oxy-5,-6,7,S-tetrahydroquinoxaline.

Exemplary phosphorylating agents which may be employed in Reaction [I] above are:

The compounds of the invention are useful as insecticides and arachnicides. They may be applied as solids or in the form of liquid sprays either in conventional type formulations, low volume or as ultra low volume applications, hereinafter referred to as LV. or U.L.V., respectively.

Solid formulations can be prepared by dissolving the active compound in a solvent, generally a relatively volatile organic solvent, such as xylene, cyclohexanone, a lower alcohol or the like, spraying the solution onto an agitated bed of inert solid carrier, such as attapulgite, kaolin, talc or diatomaceous earth in granular or finely ground form, and, thereafter, drying the thus prepared formulation. Preparation of wettable powders, which are diluted with water before spraying, usually include the addition of an emulsifier, such as an alkyl aryl sulfonate, alkyl aryl polyglycol ether, and the polyalkylene fatty acid esters. Such formulations usually contain from about 25% to 95% by weight of toxicant and are prepared with finely ground inert carrier.

In general, the liquid sprays can be prepared as concentrates by dissolving the toxicant in an organic solvent, such as xylene, benzene, lower alcohol, fuel oil, or the like, with or without an emulsifying agent, and further diluting with either water or an organic diluent, such a deodorized kerosene for application. The concentrates generally contain from about 20% to 95% by Weight of toxicant and when diluted for application may contain as little as 0.01% of active material.

The toxicant may also be diluted with a small amount of an essentially non-evaporative solvent, such as the high aromatic solvents (95% or better aromatics), having a flash point above about 125 R, such as Panasol or Socal 44L. The mixture is applied as such at Very low rates (i.e., about 1 to 32 fluid ounces per acre).

Advantageously, the compounds of the invention have activity against a wide variety of economically important plant pests. Moreover, they are highly effective as either contact or systemic pesticides and are outstanding for the control of soil insects and provide excellent control of both the larval and adult stages of both insects and arachnids. Additionally, it has been observed that the compounds of the invention are non-phytotoxic at pesticidaily effective rates.

The invention will be better understood by referring to the illustrative examples set forth below. These are not to be taken as limitative of the invention. All parts are by Weight unless otherwise stated.

EXAMPLE 1 Preparation of 2-bromo-4-methylcyclohexanone A few drops of bromine are added to a solution of 50 parts of 4-methyl-cyclohexanone, 20 parts (by volume) of glacial acetic acid and parts of water in a suitable reaction vessel. The mixture is then heated to 60 C., until all the bromine is absorbed. An additional 25 parts of bromine are then added to the stirred mixture, keeping the temperature below 60 C. The mixture is next added to ice water, extracted with methylene chloride, and the methylene chloride layer washed with potassium bicarbonate solution and dried. Evaporation of the solvent yields 84.0 parts of 2-bromo-4-methylcyclohexanone as an oil.

EXAMPLE 2 Preparation of 4-methylcyclohexane-1,2-dione A mixture of 84.0 parts of 2-bromo-4-methylcyc1ohexanone in 500 parts of water is stirred vigorously at C. for 10 minutes in a suitable reaction vessel. 125 parts of ferric chloride hexahydrate in parts of hot water are added and the reaction mixture is maintained at 95 C. for'20 minutes. It is then cooled to 40 C., saturated with ammonuim sulfate and extracted with methylene chloride. The methylene chloride layer is dried over magnesium sulfate and evaporated to yield 59.2 parts of 4- methylcyclohexane-1,2-dione as a dark red oil.

EXAMPLE 3 Preparation of 6 (7) -rnethyl-2-oxy-5,6,7,8-tetrahydroquinoxaline A mixture of 43.0 parts of 4-methylcyclohexane-L2- dioue, 60.0 parts of glycinamide hydrochloride and 100 parts of water are cooled in ice. 100 parts (by volume) of a40'% sodium hydroxide solution are added and the solution stirred for 45 minutes. It was then acidified and a gummy solid is recovered. The latter is Washed with methylene chloride and then triturated with ethanol to yield 4.5 parts of 6 (7 )-methyl-2-oxy-5,6,7,8-tetrahydroquinoxaline as a white solid, having a melting point equal to 258 C.260 C.

EXAMPLE 4 Preparation of 0,0-diethyl O-5,6,7,8-tetrah'ydro-6(7)- methyl-2-quinoxalinyl phosphorothioate 4.2 parts of 6(7)-methyl-2-oxy-5,6,7,8 tetrahydroquinoxaline are added to a solution of 4.2 parts of potassium t-butoxide in t-butanol. The mixture is cooled in an ice bath and 3.56 parts of 0,0-diethyl phosphorochloridothioate then added. After 15 minutes, the reaction mixture is poured into a mixture of ice water and methylene chloride. The methylene chloride layer is washed thoroughly with water and dried. The solvent is finally evaporated and the residue chromatographed on alumina to yield 3.30 parts of above-named product as a yellow oil.

Analysis-Calm. for C H N O PS (percent): C, 49.36; H, 6.64; N, 8.86; S, 10.15; P, 9.80. Found (pen cent): C, 50.20; H, 6.87; N, 9.97; S, 11.22; P, 10.61.

EXAMPLE 5 Preparation of 2-oxy-5,6,7,8-tetrahydroquinox-a1ine A solution of 6.0 parts of glycinamide hydrochloride and 5.0 parts of cyclohexane-1,2-dione in 50 parts of Water is cooled in-an ice bath and parts of 40% aqueous sodium hydroxide solution are added thereto. After five minutes the solution is heated and vigorously stirred at 40 C. for 1.5 hours. It is then cooled in an ice bath and 30 parts of water are added. Concentrated hydrochloric acid is added until the pH of the solution is about 5. Solid sodium bicarbonate is next added to neutralize the mixture. The solid precipitate is filtered, washed with water, and dried under vacuum to give 5.8 parts (86%) of the desired product, melting point 268 C.-270 C.

Analysis.Calcd. for C H N O (percent): C, 63.9; H, 6.70; N, 18.6. Found (percent): C, 63.7; H, 7.00; N, 18.4.

EXAMPLE 6 Preparation of 0,0-dimethyl O-5,6,7,8-tetrahydro-2- quinoxalinyl phosphorothioate A stirred solution of 5.0 parts of tetramethylene-2- pyrazinone and 3.75 parts of potassium t-butoxide in 100 parts (by volume) of t-butanol is cooled to about C. To the cooled solution is next added 5.35 parts of 0,0- dimethyl phosphorochloridothioate. Resultant mixture is stirred at room temperature for 15 minutes and then at 40 C. for an additional fifteen minutes. Water is then added and the mixture extracted with methylene chloride. The methylene chloride solution is washed several times with water, dried over magnesium sulfate, and evaporated to yield 5.6 parts of product as a dark oil identified by NMR analysis.

Analysis.Calcd. for C H N O PS (percent): C, 43.79; H, 5.47; P, 11.31. Found (percent): C, 41.81; H, 5.53; P, 10.92.

' EXAMPLE 7 Preparation of 0,0-diisopropyl 5,6,7,8-tetrahydro-2- quinoxalinyl phosphorothioate Five parts of tetrahydro-Z-keto-quinoxaline are suspended in 100 parts (by volume) of t-butanol containing 5 parts of potassium t-butoxide. The reaction mixture is refluxed for fifteen minutes, then 5.6 parts of diisopropylphosphorochloridothioate added. The reaction mixture is refluxed until a pH of 7 is attained. Water is then added and the aqueous solution is then extracted with methylene chloride. The methylene chloride solution is separated from the water and dried with magnesium sulfate and upon evaporation of the solvent, the remaining oil is taken up in petroleum ether and chromatographed on alumina. Elution is effected first with petroleum ether and then with methylene chloride to yield the above named product on removal of the solvent.

Analysis.Calcd. for C I-I N O PS (percent): C, 50.90; H, 6.97; N, 8.48; S, 9.72. Found: C, 49.09; H, 7.01; N, 8.37; S, 9.46.

EXAMPLE 8 Preparation of diisopropyl 5,6,7,8-tetrahydro-2-quinoxalinyl phosphate Following the procedure of Example 7 but substituting diisopropyl phosphorochloridate for diisopropyl phosphorochloridothioate, there is obtained the above-named product in good yield.

Analysis.Calcd. for C H N O P (percent): C, 53.51; H, 7.33; N, 8.92; P, 9.87. Found (percent): C, 53.13; H, 7.25; N, 8.75; P, 9.77.

6 EXAMPLE 9 Preparation of 0,0-diethyl O-5,6,7,8-tetrahydro-2- quinoxalinyl phosphorothioate 3 parts of tetramethylene-Z-pyrazinone are suspended in 50 parts (by volume) of t-butanol containing 3 parts of potassium t-butoxide. The reaction mixture which was previously flushed with nitrogen is refluxed for one and a half hours. Subsequently, 3 parts of diethyl phosphorochloridothioate are added slowly. Resultant reaction mixture is refluxed for one hour and then diluted with water and extracted with methylene chloride. The organic layer is then separated and evaporated under vacuum. 3.6 parts of a brown oil are collected. The oil is finally washed with cold hexane to obtain 2.8 parts of product.

Analysis.--Calcd. for C H N O PS (percent): C, 47.69; H, 6.29; N, 9.27; S, 10.61; P, 10.25. Found (percent): C, 47.51; H, 6.37; N, 9.07; S, 10.81; P, 10.27.

EXAMPLE 10 Preparation of O-ethyl O-methyl O-5,6,7,8-tetrahydro-2- quinoxalinyl phosphorothioate 5 parts of tetrahydro-2-keto-quinoxaline are suspended in parts (by volume) of t-butanol containing 5 parts of potassium t-butoxide. The reaction is refluxed for one half hour, then 5 parts of O-ethyl, O-methyl phosphorochloridothioate are added. The reaction mixture is stirred first at room temperature for one half hour, then at reflux temperature for 3 hours and left overnight at room temperature. Water is added and the mixture extracted with methylene chloride, dried, evaporated and chromatographed to obtain 4.6 parts of product.

Analysis.-Calcd. for C H N O PS (percent): C, 45.83; H, 5.90; N, 9.72; P, 10.76. Found (percent): C, 45.65; H, 6.13; N, 9.97; P, 10.53.

EXAMPLE 11 Preparation of N,N-dimethyl-O-ethyl O-5,6,7,8-tetrahydro-2-quinoxaylinyl phosphoroamidothioate 5.0 par-ts of tetrahydro-2-keto-quinoxaline and 3.8 parts of potassium t-butoxide are dissolved in about 100 parts (by volume) of dimethylsulfoxide and cooled to 10 C. 6.3 parts of O-ethyl-N-dimethyl phosphorochloridoamidate are added to the mixture and held under agitation at room temperature for one-half hour. It is then extracted with methylene chloride, and the organic layer washed with water and dried to yield 7.5 parts of a yellow oil.

Analysis.Calcd. for C H PN SO' (percent): C, 47.9; H, 6.68; N, 13.97; S, 10.63; P, 10.29. Found (percent): C, 48.06; H, 6.83; N, 14.04; S, 10.62; P, 10.25.

EXAMPLE 12 Preparation of O-ethyl O-5,6,7,8,-tetrahydro 6(7)- methyl-Z-quinoxalinyl phenylphosphonothioate To a stirred solution of 5 parts of tetramethylene-2- pyrazinone and 3.8 parts of potassium t-butoxide in parts (by volume) of dimethylsulfoxide at about 10 C. are added 3.8 parts of O-ethyl phenylphosphonochoridothioate. The mixture is worked up, as in Example 11, to yield 5.5 parts of a yellow oil.

Analysis.CalCd. for C H PN SO (percent): C, 57.5; H, 5.72; N, 8.39; S, 9.58; P, 9.27. Found (percent): C, 57.72; H, 5.68; N, 8.15; S, 9.82; P, 9.26.

EXAMPLE 13 Preparation of O,S-Dimethyl O5,6,7,8-tetrahydro-2- quinoxalinyl phosphorodithioate 5 parts of 5,6,7,8-tetrahydro-2-keto-quinoxaline are suspended in 100 parts (by volume) of t-butanol containing 5 parts potassium t-butoxide. To this mixture, after stirring at reflux for /2 hour, are added five parts of O,S-dimethyl phosphorochloridodithioate. The reaction mixture is stirred at room temperature for sixteen hours and then refluxed for one-half hour. Then water is added and the reaction mixture extracted with methyl ene chloride. The methylene chloride layer is dried over magnesium sulfate and evaporated to dryness. The dark oil is taken up in petroleum ether and the formed solids are filtered and the filtrate chromatographed on alumina. Elution with petroleum ether and methylene chloride yields 2.5 parts of pure product, analyzing in percent as:

Calcd. for C H N O PS (percent): C, 41.36; H, 5.17; N, 9.65; S, 22.12; P, 10.68. Found (percent): C, 40.96; H, 5.35; N, 8.17; S, 18.26; P, 8.93.

EXAMPLE 14 Preparation of O-ethyl-O-5,6,7,8-tetrahydro-2-quinoxalinyl ethanephosphonate To a stirred suspension of parts of tetramethylene- 2-pyrazinone and 3.8 parts of potassium t-butoxide in 150 parts (by volume) of t-butanol which had been stirred for one hour at room temperature, are added 5.23 parts of ethyl ethanephosphonochloridate. Reaction occurred immediately and the mixture is worked up and then washed with cold n-hexane yielding 6.5 parts of yellow oil. This is taken up in hot hexane, treated with a small amount of alumina, then with charcoal, filtered while still hot, and concentrated leaving 5.2 parts of product whose index of refraction (11 is 1.5128 and analyzmg as:

Calcd. for C H PN O (percent): C, 53.3; H, 7.08; N, 10.36; P, 11.44. Found (percent): C, 52.96; H, 6.83; N, 10.22; P, 11.29.

EXAMPLE 15 Preparation of S,S-dimethyl O5,6,7,8,-tetrahydro-2- quinoxalinyl phosphorodithioate 5.0 parts of tetramethylene-2-pyrazinone and 3.75 parts of potassium t-butoxide in 250 parts (by volume) of t-butanol are stirred at room temperature for two hours. 5.9 parts of S,S-dimethyl phosphorochloridothioate are then added and the mixture immediately treated with methylene chloride, washed with water and dried to yield 8.3 parts of yellow oil. The latter is washed with ice-cold hexane, taken up in a hot benzene-hexane mixture, treated with charcoal, filtered and concentrated to yield 5.5 parts of an orange oil.

Analysis.--Calcd. for C H PN S O (percent): C, 41.4; H, 5.21; N, 9.65; S, 22.05; P, 10.65. Found (percent): C, 41.15; H, 5.20; N, 9.42; S, 22.12; P, 10.59.

EXAMPLE 16 Preparation of -O-isopropyl O-methyl O5,-6,7,8-tetrahydro-2-quinoxalinyl phosphorothioate 2.5 parts of potassium t-butoxide are dissolved in 100 parts (by volume) of t-butyl-alcohol and added to a stirred solution of 3.0 parts of tetramethylene-Z-pyrazinone in t-butanol. The mixture is stirred until a clear brown solution is formed in about 15 minutes at 45 C. When the mixture has been cooled to about 40 C., 3.7 parts of O-isopropyl O-methyl phosphorochloridothioate in t-butanol are added all at once. This mixture is partitioned between 100 parts of water and 100' parts (by volume) of methylene chloride.

The water layer is extracted with 50 parts (by volume) of methylene chloride, and the combined layers washed with 50 parts of water, followed by aqueous 1% sodium bicarbonate and then again with water. After drying over sodium sulfate and filtered to remove solvent, 4.5 parts of brown oil are obtained.

Analysis.-Calcd. for PN SO C H (percent): C, 47.67; H, 6.33; N, 9.27; P, 10.25; S, 10.61. Found (percent): C, 47.31; H, 6.70 N, 10.21; P, 10.26; S, 10.88.

8 EXAMPLE 17 Preparation of diethyl 5,6,7,8-tetrahydro-2-quinoxalinyl phosphate 10 parts of tetramethylene-Z-pyrazinone are dissolved in 300 parts (by volume) of t-butanol containing 10 parts of potassium t-butoxide and reacted with 10 parts of diethyl phosphorochloridate. The mixture is stirred for two hours, then refluxed for 20 minutes and allowed to cool. Water is added to dissolve the resultant solid and the solution is extracted therefrom with methylene chloride. The methylene chloride layer is separated from the water, dried over magnesium sulfate and concentrated to obtain the desired product which analyzes as:

Calcd. for C H N O P (percent): C, 50.37; H, 6.64; N, 9.79; P, 10.83. Found (percent): C, 50.50; H, 6.60; N, 9.90; P, 10.70.

EXAMPLE 18 Preparation of 0,0-dipropyl O5,6,7,S-tetrahydroquinoxalinyl phosphorothioate 5 parts of tetramethylene-Z-pyrazinone are suspended in parts of t-butanol containing 5 parts of potassium t-butoxide. The reaction mixture is refluxed for one-half hour. 5 parts of di-n-propyl phosphorochloridothioate are then added. Resultant reaction mixture is refluxed for another two hours, water then added and the solution extracted with methylene chloride. The methylene chloride solution is dried over magneslum sulfate and evaporated to dryness. The oil which remains is taken up in petroleum ether. The solution is filtered to remove starting material and the petroleum ether solution chromatographed on alumina. Elution of the above solution with methylene chloride and subsequent removal of solvent yields the desired product which analyzes as:

Calcd. for C H N O PS (percent): C, 50.90; H, 6.97; N, 8.48; S, 9.72; P, 9.39. Found (percent): C, 50.80; H, 7.00 N, 8.37; S, 9.65; P, 9.19.

EXAMPLE 19 The insecticidal activity of typical compounds of the invention is demonstrated by the following tests wherein graded levels of toxicant are used for controlling a variety of insect species. Test procedures as well as the results obtained are set forth below:

Bean aphid-Aphis fabae Scopoli Compounds are tested as 0.1%, 0.01% and 0.001% solutions or suspensions in 65% acetone-35% water. Two-inch fiber pots, each containing a nasturtium plant about two inches high and infested with about aphids two days earlier are sprayed with the test solutions so as to give complete coverage of the aphids and the plants. The sprayed plants are laid on their sides on white enamel trays which have had the edges coated with oil as a barrier. Mortality estimates are made after holding for two days at 70 F., and 50% RH.

Activity reported in Table I as percent kill of insects.

onaone o-f TABLE I-Continued Aphids Structure .1% .01% .001%

H N (GzHsOhP-OT I 100 100 100 C3H O\fi N (CHmN I 0 II N CaH1O)zPO-f 100 100 40 H N a )2P0 100 100 100 H N (n-CaH1O)2PO 100 100 100 CzH50\fi N 0 II N (CHsS)zP-O 100 100 100 CHaS\fi N /PO 100 100 50 crrao CH O\4[Zi) N c2H50 fi N /PO n 100 100 100 s II N (C2H5O)2PO 100 100 100 s H N (CHghCHO-P-O 100 100 100 CHafB Southern armywormPr0denia eridania (Cramer) The solutions from the aphid test above are also used for this test. Sieva lima bean primary leaves are dipped for three seconds in the test solution and set in a hood on a screen to dry. When dry, each leaf is placed in a 4'inch petri dish which has a moist filter paper in the bottom with ten third-instar armyworm larvae about /s" long. The dishes are covered and held at F., and 60% RH. After 2 days, mortality counts and estimates of the amount of feeding are made.

Activity is reported in Table II as percent kill obtained with each level of toxicant.

TABLE II Southern Armyworm Structure .1% .01% .001%

S 100 100 II N (C2H O)zPO( S 100 40 II N (CH O)2PO- O 100 100 90 I] N (canon-0T S 100 100 0 H N n-oamonP-of C2H5 O\fi N 100 100 100 /PO CHaO CH3S\fi N 100 70 O /P-O CHaO CzHsO S 100 100 20 \ll 0 N C2H60\fi N 100 100 0 T S 100 100 0 II N (C2H O)2P0 Confused flour beetle (TC)-Trib0 lium confuuum Jacquelin duVal grinding with a mortar and pestle until dry. 125 mg. of this 1% dust are then blown into the top of a dust settling tower. The dust is allowed to settle on four-inch petri dishes for two minutes, giving a deposit of approximately 87 rug/sq. foot of the 1% dust. The dishes are removed and 25 adult confused flour beetles are added immediately. The dishes are held for three days at 80 F. and 60% RH, following which mortality counts are made.

Large milkweed bug (MB)-Oncopeltus fasciatus Dallas The 1% dusts described above are used in this test.

The 1% dust is springled evenly over the glass bottom German cockroach (GC)-Blattella germam'ca (Linnaeus) The procedure is the same as for the large milkweed bug test, except that in this test only adult males are used.

Data are reported in Table III as percent kill of insects at the level of t-oxicant employed.

TABLE III Structure TC, 1% MB, 1% GO, 1%

S 100 100 100 ll mmonP-bs 100 100 100 n N amour-T 100 100 100 n N (CzH50)zP-O u ,N ammoni -0T n N i-oaulonr-oT ammoni -of n In addition to the above tests, aqueous/acetone solutions containing either 100' ppm. or 0.1% of a test compound are applied to leaves of cotton plants. The leaves are permitted to dry, placed in petri dishes on a moist filterpaper a'nd'infested with Lygus"line0laris, Anthonomus grandis or Heliothis virescens. The petri dishes are then placed in a constant temperature room held at F. and 60% RH. for two days. After two days, mortality counts are made and percent kill of insects recorded. Further, it has been found that the compounds of the present invention exhibit residual activity against the above-mentioned cotton pests.

The results are tabularized in Table IV below.

TABLE IV Lygus, Anthono- Heliop.p.m. mus, -p.p.m. th1s,p.p.m. Structure 100 100 100 S 70 l] N (C2 50)2PO( g N 100 100 (CH O)zP-OF f N 100 90 100 (C2HsO)2PO N 021150 S 8D 10B 100 i o /N\ CH3O/ To show the eifectiveness against common malaria mosquito, Anopheles quadrimaculatus, test compounds are prepared as 10 ppm. and 1.0 p.p.m. solutions in acetone and coated on a hard surface accessible to contact by 4- to 5-day old mosquitoes of mixed sexes. A sugar solution is provided as food for the mosquitoes which are caged for 24 hours in such manner as to permit exposure of the mosquitoes to the treated surface. After the 24 hour period, mortality counts are made and the results recorded.

Test results are tabulated in Table V below.

TABLE V--Continued TABLE VI-Continued Mosquito, Adults. Fly Structure P.p.m. 10 P.p.m.1

\ P.p.m. P.p.m. P.p.m ;.H 0 8 Structure 50 5 .5

i 0 /N 100 100 5 I i N 100 100 0 CH3) (n-OsH O)2PO I OH s s i \n N 10 \N A 33 021150 s 100 100 60 CHIO lL \N CHaO 0,11 0 v \n N 0 0 \N T 1 0 (R 100 12 o omsnP-o /N s u ,N 0 N/ CH outs s 100 0 P-0 /N \N CHsO l s n /N 0 100 \N (CH)'CHO P 10 021150 0 100 100 100 CH:() ii 0 /N \N 0 emf f \N To demonstrate the efiectiveness against the housefly, CZHO S 100 0 Musca domestica Linnaeus, groups of 25 adult female /N houseflies are placed in wide-mouth pint mason jars, and covered with a screen cap. The test compounds are for- Q mulated as an emulsion containing 1000 p.p.m. of test materials, an emulsifier, acetone, and water. This emulsion is diluted with 10% sugar solution, giving a concentration E N 100 0 of 50, 5 or 0.5 p.p.m. The solution is placed so that the 40 (Gamma-o flies can feed on it through the screen. Mortality counts are made after two days at 80 F. \N

Results obtained are reported in Table VI below.

s 100 100 56 II N TABLE VI (CHshCHO-P-O Fly CHfl I P.p.m. P.p.m. P.p.m: N Structure 6 .5

fir, 100 100 20 50 (mmohr-O-( \N EXAMPLE 20 s 100 100 24 AL The systemic actlvrty of the compounds of the invention is demonstrated by the following tests. The compound to be tested is formulated as an emulslon containing test material, an emulsifier, acetone, and 0 100 m0 100 water. This is diluted with water to give 100, 10 or 1 u /N p.p.m. of toxicant in test. A sieva lima bean plant with s )2 only the primary leaves unfolded is cut off just above the soil level and inserted into a bottle of test emulsion and held in place by a bit of cotton wrapped around the stem. 6 The bottle is then placed in a ventilated 'box with the II N 100 m0 9 leaves extending outside the box, such that any possible (i-C HyOhP-O fumes from the compound will be drawn out the end of the box rather than rising to atfect the test leaves. About \N 50 adult two-spotted spider mites are placed on each leaf.

7 After holding three days at 80 F. and 60% R.H., mor- 100 33 12 tality estimates are made and one leaf from each plant is placed on a moist filter paper in the bottom of a petri dish. Ten third-instar southern armyworm larvae are added to each dish and mortality counts are made after holding another three days at F. and 60% RH.

TABLE Vfr Systemics Mites Southern Armyworm Structure '$b i -ig .p.n 1 P411111.

3 100 100 100 70 o (CaHO)2I O-[ l g N 100 100 o 100 100 0 (Groom-0T W (I? N 100 100 100 100 90 (amour-0T 021150 s 100 as o 100 100 0 N lLO CHaO 021350 I? N 100 90 0 100 o 0 P-O czHs is, N 90 v u mo vso (CzH O)zPO 1 CH3 I t i N 100 04 (oHowHo-g-o EXAMPLE 21 Arachnicidal activity of the compounds of the invention is demonstrated against the two-spotted spider mite, Tetranychus urticae (Koch). r

Sieva. lima bean plants with primary leaves three to four TABLE VIIIContin'ue'd inches long are infested with about 100 adult mites per leaf four hours before use in this test. The mite and egg Mtes infested plants are dipped for three seconds in 0.1, 0.01 or structure .10% .001% 0.001% solutions of test compound, and the plants set in S 100 m0 100 the hood to dry. They are held for two days at 80 F., (CH 0) iL N RH, and the adult mite mortality estimated on one a 2 leaf under a stereoscopic microscope. The other leaf is left on the plant an additional five days and then examined at 10X power to estimate the kill of eggs and of newly- .J mo m0 100 hatched nymphs, giving a measure of ovicidal and residual 60 u N action, respectively. Solutions are made in acetone"- (CzHsOhPA) 35% water and the results are reported in tabular form in Table VIII below. \N I 4 65 02B 0 a y l 7 19g 100 0 TABLE vm 0 Mites (CHa):N Structure v. N r. r. t t. 100 100 s1 '0 0 0 TABLE VII[Continued Mites Structure 1% 01% 001% i N 100 0 (i-C=H)2P-Or s 100 o 0 H N (n-CaHfihP-Of CzH50\fi N 100 100 79 0 H N 100 100 0 (omsnP-of CHzS\fi N 100 0 0 1 -0 CHaO \[I N P-O 02115 O2H5O\S 100 100 60 ll N D s 100 100 2 II N (C:H50)2P-O s 100 100 100 I] N (CHa)2GHO-PO CHfl EXAMPLE 22 Larvicidal activity of the compounds of the invention is shown in the following tests against the larvae of the malaria mosquito.

Common malaria mosquito-Anopheles quadrimacularus Say larvicide test Groups of 25 larvae of the common malaria mosquito are placed in a 50ml. beaker containing '25 m1. of water. The test compound is formulated as an emulsion containing .4 or .1 p.p.m. of test material, emulsifier, acetone, and water. The larvae in 25 ml. of water are added and mortality counts are made after 24 hours at 80 F. and recorded in Table IX.

TABLE IX Mosquito, fiarvae, Structure p.p.m. .4 p.p.m. .1

i N 100 100 (CzH O)2PO i /N\ 100 100 (CH O)2PO v (11]) N 100 0 (C2H O)2POE E N 100 20 (n-oamo P-of I) C2H50\fi N 100 100 P-O CHsO I) OHaS\fi N 0 P-O CHaO C2H O\(]? N 0 P-O CzHs K D C2H50\fi N 100 5 N cznsoni -of EXAMPLE 23 Mortality counts are made after six days at 80 TABLE X-Continued Rootworms, Wireworms,

Lbs/Acre Lbs/Acre Structure 50 W 10 50 "'10 TABLE x OZHSO s 100 75 55 Rootworxns, Wireworms, II N Lbs/Acre Lbs/Acre PO Structure 50 50 10 m \N E N 109 100 100 100 10 H (O2H5O)2P O i N 100 100 100 80 (C H5O)aPO CH a i 100 85 100 100 N (CHaO)2P 0 i N 100 100 100 100 (CH3)2OHO1{O \N C1130 4])I N 100 85 100 100 ozmonr-o What is claimed is:

. 1. A tetrahydroquinoxalinyl compound of the formula:

\N N Iii/R1 100 65 90 0 1-c31110 21 -o l R2 wherein X is a member selected from the group consisting of sulfur and oxygen; R and R are each lower alkyl, N 100 m0 100 60 lower alkoxy; lower thioalkyl, phenyl, halophenyl, benzyl (i-CzH10)zi-O or NR R R is hydrogen or lower alkyl; and R and R are each selected from the group consisting of hydrogen and lower alkyl.

N 2. The compound according to claim 1: 0,0-diethyl s 100 100 100 100 O 5,6,7 ,8 tetrahydro 6( 7 )-methyl-2-quinoxalinyl phosi /N phorothioate.

, a 3. The compound according to claim 1: 0,0-dimethyl O,5,6,7,8-tetrahydro-2-quinoxalinyl phosphorothioate. \N 4. The compound according to claim 1: 0,0-diisopropyl CQHSO S 100 100 m0 m0 5,6,7,8-tetrahydro-2-quinoxalinyl phosphorothioate.

U '5. The compound according to claim 1: diisopropyl 5,6, 7,8-tetrahydro-2-quinoxalinyl phosphate. 6. The compound according to claim 1: 0,0-diethyl O-5,6,7,8-tetrahydro-2-quinoxalinyl phosphorothioate. CH S S 100 40 7. The compound according to claim 1: O-ethyl O- a \H /N methyl O-5,6,7,8-tetrahydro-2-quinoxalinyl phosphorothioate. OHiO T n References Cited N UNITED STATES PATENTS o2H50\( N 100 3,150,149 9/1964 Uhlenbroek et al. 260-250 f 55 NICHOLAS s. RIZZO, Primary Examiner 02115 US. Cl. X.R. 

